Evidence map›Paper›PMID 36215333›Full record

ArticlePLoS computational biology2022

Experimental guidance for discovering genetic networks through hypothesis reduction on time series.

Breschine Cummins, Francis C Motta, Robert C Moseley, Anastasia Deckard, Sophia Campione, Marcio Gameiro, Tomáš Gedeon, Konstantin Mischaikow, Steven B Haase

Abstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Evolution of the Cell-Cycle Clock Models: Biochemical or Transcriptional?Advances in experimental medicine and biology · 2026
    Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Breschine CumminsDepartment of Mathematical Sciences, Montana State University, Bozeman, Montana, United States of America.ORCID 0000-0002-3097-5277
Francis C MottaDepartment of Mathematical Sciences, Florida Atlantic University, Boca Raton, Florida, United States of America.ORCID 0000-0002-0364-5440
Robert C MoseleyDepartment of Biology, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-4615-457X
Anastasia DeckardGeometric Data Analytics, Durham, North Carolina, United States of America.ORCID 0000-0003-1142-5357
Sophia CampioneDepartment of Biology, Duke University, Durham, North Carolina, United States of America.
Marcio GameiroDepartment of Mathematics, Rutgers University, New Brunswick, New Jersey, United States of America.
Tomáš GedeonDepartment of Mathematical Sciences, Montana State University, Bozeman, Montana, United States of America.
Konstantin MischaikowDepartment of Mathematics, Rutgers University, New Brunswick, New Jersey, United States of America.
Steven B HaaseDepartment of Biology, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0001-8127-8992

Funding

Needle in a haystack: effective search for dynamics across the space of networksR01GM126555 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI MISCHAIKOW, KONSTANTIN · 2017 to 2021
$1.8M
NIGMS NIH HHS R01 GM126555
6 · The paper itself

Abstract

Large programs of dynamic gene expression, like cell cyles and circadian rhythms, are controlled by a relatively small "core" network of transcription factors and post-translational modifiers, working in concerted mutual regulation. Recent work suggests that system-independent, quantitative features of the dynamics of gene expression can be used to identify core regulators. We introduce an approach of iterative network hypothesis reduction from time-series data in which increasingly complex features of the dynamic expression of individual, pairs, and entire collections of genes are used to infer functional network models that can produce the observed transcriptional program. The culmination of our work is a computational pipeline, Iterative Network Hypothesis Reduction from Temporal Dynamics (Inherent dynamics pipeline), that provides a priority listing of targets for genetic perturbation to experimentally infer network structure. We demonstrate the capability of this integrated computational pipeline on synthetic and yeast cell-cycle data.

Indexed as

Gene Regulatory NetworksTranscription FactorsSaccharomyces cerevisiaeTime FactorsTranscription Factors

Identifiers

PMID36215333
PMCPMC9584434

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.